TMEM171 (transmembrane protein 171) - Rat Genome Database

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Gene: TMEM171 (transmembrane protein 171) Homo sapiens
Analyze
Symbol: TMEM171
Name: transmembrane protein 171
RGD ID: 1606157
HGNC Page HGNC:27031
Description: Predicted to be located in membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: proline-rich protein PRP2; PRP2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38573,120,575 - 73,131,809 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl573,120,569 - 73,131,809 (+)EnsemblGRCh38hg38GRCh38
GRCh37572,416,402 - 72,427,636 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36572,452,158 - 72,463,397 (+)NCBINCBI36Build 36hg18NCBI36
Celera568,311,763 - 68,323,014 (+)NCBICelera
Cytogenetic Map5q13.2NCBI
HuRef567,622,070 - 67,633,327 (+)NCBIHuRef
CHM1_1571,849,116 - 71,860,378 (+)NCBICHM1_1
T2T-CHM13v2.0573,601,908 - 73,613,146 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
(-)-epigallocatechin 3-gallate  (EXP)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (EXP)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-palmitoylglycerol  (EXP)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
7,9-dihydro-1H-purine-2,6,8(3H)-trione  (EXP)
acetamide  (ISO)
acrylamide  (ISO)
aflatoxin B1  (EXP)
ammonium chloride  (ISO)
antirheumatic drug  (EXP)
aristolochic acid A  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[b]fluoranthene  (ISO)
bisphenol A  (ISO)
bisphenol F  (EXP)
butanal  (EXP)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
calcium silicate  (ISO)
carbon nanotube  (ISO)
chromium(6+)  (EXP)
chrysene  (ISO)
CU-O LINKAGE  (EXP)
dexamethasone  (EXP)
dibenz[a,h]anthracene  (ISO)
dichloroacetic acid  (ISO)
dioxygen  (EXP)
diquat  (ISO)
ethanol  (ISO)
folic acid  (ISO)
fonofos  (EXP)
gentamycin  (ISO)
indole-3-methanol  (ISO)
indometacin  (EXP)
lipopolysaccharide  (EXP)
N-nitrosodiethylamine  (ISO)
nickel sulfate  (EXP)
nitrofen  (ISO)
paraquat  (ISO)
parathion  (EXP)
PCB138  (ISO)
pentanal  (EXP)
perfluorononanoic acid  (EXP)
perfluorooctanoic acid  (ISO)
pirinixic acid  (ISO)
potassium chromate  (EXP)
pregnenolone 16alpha-carbonitrile  (ISO)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
silicon dioxide  (EXP)
sodium arsenite  (EXP,ISO)
succimer  (ISO)
temozolomide  (EXP)
terbufos  (EXP)
tetrachloromethane  (ISO)
tetraphene  (ISO)
thioacetamide  (ISO)
titanium dioxide  (ISO)
tributylstannane  (ISO)
trichloroethene  (ISO)
trovafloxacin  (ISO)
valproic acid  (EXP)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
membrane  (IEA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12044878   PMID:12477932   PMID:15146197   PMID:15489334   PMID:16344560   PMID:17207965   PMID:22797727   PMID:23263486   PMID:25416956   PMID:26186194   PMID:28514442   PMID:33961781  


Genomics

Comparative Map Data
TMEM171
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38573,120,575 - 73,131,809 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl573,120,569 - 73,131,809 (+)EnsemblGRCh38hg38GRCh38
GRCh37572,416,402 - 72,427,636 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36572,452,158 - 72,463,397 (+)NCBINCBI36Build 36hg18NCBI36
Celera568,311,763 - 68,323,014 (+)NCBICelera
Cytogenetic Map5q13.2NCBI
HuRef567,622,070 - 67,633,327 (+)NCBIHuRef
CHM1_1571,849,116 - 71,860,378 (+)NCBICHM1_1
T2T-CHM13v2.0573,601,908 - 73,613,146 (+)NCBIT2T-CHM13v2.0
Tmem171
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391398,822,744 - 98,832,142 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1398,822,743 - 98,831,342 (-)EnsemblGRCm39 Ensembl
GRCm381398,686,236 - 98,695,654 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1398,686,235 - 98,694,834 (-)EnsemblGRCm38mm10GRCm38
MGSCv371399,456,193 - 99,464,786 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361399,786,395 - 99,794,988 (-)NCBIMGSCv36mm8
Celera13102,345,922 - 102,354,526 (-)NCBICelera
Cytogenetic Map13D1NCBI
cM Map1352.13NCBI
Tmem171
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8231,769,486 - 31,779,358 (-)NCBIGRCr8
mRatBN7.2230,035,278 - 30,045,996 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl230,035,278 - 30,045,049 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx237,093,085 - 37,106,136 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.022,313,122 - 2,326,173 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0230,003,666 - 30,013,446 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0228,791,831 - 28,802,135 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl228,791,875 - 28,801,223 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0247,889,908 - 47,900,063 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4229,301,092 - 29,310,650 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1229,221,460 - 29,231,019 (-)NCBI
Celera226,071,073 - 26,080,320 (-)NCBICelera
Cytogenetic Map2q12NCBI
Tmem171
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542527,457,185 - 27,464,513 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495542527,457,245 - 27,466,484 (-)NCBIChiLan1.0ChiLan1.0
TMEM171
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2442,183,385 - 42,194,835 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1540,337,014 - 40,348,485 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0542,181,966 - 42,193,088 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1542,781,305 - 42,789,684 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl542,781,305 - 42,789,684 (-)Ensemblpanpan1.1panPan2
TMEM171
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1256,036,463 - 56,044,443 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl256,037,975 - 56,044,464 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha253,008,185 - 53,018,390 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0256,558,208 - 56,566,307 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl256,559,817 - 56,566,307 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1253,617,060 - 53,627,212 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0254,384,978 - 54,395,341 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0255,275,830 - 55,286,629 (+)NCBIUU_Cfam_GSD_1.0
Tmem171
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213187,446,269 - 187,455,734 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365493,403,222 - 3,412,348 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365493,403,250 - 3,411,897 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TMEM171
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl282,287,158 - 82,297,856 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1282,287,211 - 82,297,855 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2283,995,709 - 84,006,354 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TMEM171
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1467,463,098 - 67,476,538 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl467,462,987 - 67,475,326 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604916,230,129 - 16,241,665 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tmem171
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046249052,167,045 - 2,177,234 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046249052,167,147 - 2,176,964 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TMEM171
18 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5p15.33-q13.3(chr5:22149-74412725)x3 copy number gain See cases [RCV000138780] Chr5:22149..74412725 [GRCh38]
Chr5:22149..73708550 [GRCh37]
Chr5:75149..73744306 [NCBI36]
Chr5:5p15.33-q13.3		 pathogenic
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
NM_173490.8(TMEM171):c.535G>C (p.Val179Leu) single nucleotide variant Inborn genetic diseases [RCV003264590] Chr5:73123908 [GRCh38]
Chr5:72419735 [GRCh37]
Chr5:5q13.2		 uncertain significance
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
NM_173490.8(TMEM171):c.459A>G (p.Ser153=) single nucleotide variant not provided [RCV000973185] Chr5:73123832 [GRCh38]
Chr5:72419659 [GRCh37]
Chr5:5q13.2		 benign
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32		 uncertain significance
GRCh38/hg38 5q11.2-13.2(chr5:58785203-73519962)x1 copy number loss Intellectual disability [RCV000984869] Chr5:58785203..73519962 [GRCh38]
Chr5:5q11.2-13.2		 likely pathogenic
GRCh37/hg19 5q13.2(chr5:71721970-72431813)x3 copy number gain not provided [RCV000846431] Chr5:71721970..72431813 [GRCh37]
Chr5:5q13.2		 uncertain significance
GRCh37/hg19 5q13.2(chr5:71721970-72431813)x3 copy number gain not provided [RCV000846432] Chr5:71721970..72431813 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.121A>T (p.Ile41Phe) single nucleotide variant Inborn genetic diseases [RCV003264493] Chr5:73123494 [GRCh38]
Chr5:72419321 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.416A>T (p.Asn139Ile) single nucleotide variant Inborn genetic diseases [RCV002817101] Chr5:73123789 [GRCh38]
Chr5:72419616 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.130T>C (p.Phe44Leu) single nucleotide variant Inborn genetic diseases [RCV002818466] Chr5:73123503 [GRCh38]
Chr5:72419330 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.466C>G (p.Arg156Gly) single nucleotide variant Inborn genetic diseases [RCV002762243] Chr5:73123839 [GRCh38]
Chr5:72419666 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.314A>C (p.Glu105Ala) single nucleotide variant Inborn genetic diseases [RCV002758279] Chr5:73123687 [GRCh38]
Chr5:72419514 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.179A>G (p.Lys60Arg) single nucleotide variant Inborn genetic diseases [RCV002984698] Chr5:73123552 [GRCh38]
Chr5:72419379 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.296G>T (p.Arg99Leu) single nucleotide variant Inborn genetic diseases [RCV002892377] Chr5:73123669 [GRCh38]
Chr5:72419496 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.647C>T (p.Ser216Leu) single nucleotide variant Inborn genetic diseases [RCV002767847] Chr5:73128396 [GRCh38]
Chr5:72424223 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.449C>T (p.Thr150Ile) single nucleotide variant Inborn genetic diseases [RCV002896533] Chr5:73123822 [GRCh38]
Chr5:72419649 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.266T>C (p.Leu89Pro) single nucleotide variant Inborn genetic diseases [RCV002961480] Chr5:73123639 [GRCh38]
Chr5:72419466 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.257G>T (p.Arg86Leu) single nucleotide variant Inborn genetic diseases [RCV002669351] Chr5:73123630 [GRCh38]
Chr5:72419457 [GRCh37]
Chr5:5q13.2		 uncertain significance
NM_173490.8(TMEM171):c.382G>A (p.Val128Ile) single nucleotide variant Inborn genetic diseases [RCV002878718] Chr5:73123755 [GRCh38]
Chr5:72419582 [GRCh37]
Chr5:5q13.2		 likely benign
NM_173490.8(TMEM171):c.96G>T (p.Leu32Phe) single nucleotide variant Inborn genetic diseases [RCV003205702] Chr5:73123469 [GRCh38]
Chr5:72419296 [GRCh37]
Chr5:5q13.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:86
Count of miRNA genes:47
Interacting mature miRNAs:48
Transcripts:ENST00000287773, ENST00000454765
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 711 668 20 336 21 51 8 13 193 53 707 4 1
Low 396 123 501 472 268 394 2125 330 1774 194 652 501 83 84 1277 1 1
Below cutoff 992 2050 502 122 724 41 1858 1404 1848 26 591 371 86 1 989 1241 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000287773   ⟹   ENSP00000287773
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl573,120,569 - 73,131,809 (+)Ensembl
RefSeq Acc Id: ENST00000454765   ⟹   ENSP00000415030
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl573,120,575 - 73,131,809 (+)Ensembl
RefSeq Acc Id: NM_001161342   ⟹   NP_001154814
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38573,120,575 - 73,131,809 (+)NCBI
GRCh37572,410,286 - 72,427,765 (+)NCBI
Celera568,311,763 - 68,323,014 (+)RGD
HuRef567,622,070 - 67,633,327 (+)RGD
CHM1_1571,849,116 - 71,860,378 (+)NCBI
T2T-CHM13v2.0573,601,908 - 73,613,146 (+)NCBI
Sequence:
RefSeq Acc Id: NM_173490   ⟹   NP_775761
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38573,120,575 - 73,131,809 (+)NCBI
GRCh37572,410,286 - 72,427,765 (+)NCBI
Build 36572,452,158 - 72,463,397 (+)NCBI Archive
Celera568,311,763 - 68,323,014 (+)RGD
HuRef567,622,070 - 67,633,327 (+)RGD
CHM1_1571,849,116 - 71,860,378 (+)NCBI
T2T-CHM13v2.0573,601,908 - 73,613,146 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011543156   ⟹   XP_011541458
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38573,120,575 - 73,131,809 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054351625   ⟹   XP_054207600
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0573,601,908 - 73,613,146 (+)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_001154814   ⟸   NM_001161342
- Peptide Label: isoform 2
- UniProtKB: Q8WVE6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_775761   ⟸   NM_173490
- Peptide Label: isoform 1
- UniProtKB: Q8N0S1 (UniProtKB/Swiss-Prot),   Q8TDT7 (UniProtKB/Swiss-Prot),   Q8WVE6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011541458   ⟸   XM_011543156
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000415030   ⟸   ENST00000454765
RefSeq Acc Id: ENSP00000287773   ⟸   ENST00000287773
RefSeq Acc Id: XP_054207600   ⟸   XM_054351625
- Peptide Label: isoform X1

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8WVE6-F1-model_v2 AlphaFold Q8WVE6 1-324 view protein structure

Promoters
RGD ID:6869862
Promoter ID:EPDNEW_H8096
Type:initiation region
Name:TMEM171_1
Description:transmembrane protein 171
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38573,120,575 - 73,120,635EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:27031 AgrOrtholog
COSMIC TMEM171 COSMIC
Ensembl Genes ENSG00000157111 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000287773 ENTREZGENE
  ENST00000287773.5 UniProtKB/Swiss-Prot
  ENST00000454765 ENTREZGENE
  ENST00000454765.7 UniProtKB/Swiss-Prot
GTEx ENSG00000157111 GTEx
HGNC ID HGNC:27031 ENTREZGENE
Human Proteome Map TMEM171 Human Proteome Map
InterPro TMEM171 UniProtKB/Swiss-Prot
KEGG Report hsa:134285 UniProtKB/Swiss-Prot
NCBI Gene 134285 ENTREZGENE
PANTHER PTHR31617 UniProtKB/Swiss-Prot
  TRANSMEMBRANE PROTEIN 171 UniProtKB/Swiss-Prot
Pfam TMEM171 UniProtKB/Swiss-Prot
PharmGKB PA162405933 PharmGKB
UniProt Q8N0S1 ENTREZGENE
  Q8TDT7 ENTREZGENE
  Q8WVE6 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary Q8N0S1 UniProtKB/Swiss-Prot
  Q8TDT7 UniProtKB/Swiss-Prot